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46篇 您的检索式：作者名="Ceulemans L"

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	题名	作者	年代	出处	被引量
1	A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy显示文摘	Audenaert D CLAES L Ceulemans	2003	Neurology2003，61，6：	1
2	Clinical experience with levetira-ce-tam in childhood epilepsy:an add-on and mono-therapy trial显示文摘	Lagae L Buyse G Ceulemans B		0，，：	1
3	Clinical experience with levetiracetam in childhood epilepsy: an add-on and mono- therapy trial显示文摘	Lagae L Buyse G Ceulemans B	2005	Seizure2005，14，1：	1
4	Early myoclonic encephalopathy caused by a disruption of the neuregulin- 1 re-ceptor ErbB4 显示文摘	Backx L Ceulemans B Vermeesch JR	2009	Eur J Hum Genet2009，17，3：	1
5	New insights in in- testinal ischemia-reperfusion injury: implications for intestinal trans- plantation 显示文摘	Lenaerts K Ceulemans L J Hundscheid 1I-1	2013	Curt OpinOrgan Transplant2013，18，3：	1
6	Effects of ozoneexposure in open-top chambers on poplar ( Populus nigra) andbeech ( Fagus sylvatica ) : a comparison 显示文摘	Border K De Temmerman L Ceulemans R	2000	EnvironmentalPollution2000，109，3：	1
7	A deletion in SCN1B is associated with febrile seizures and early - onset absence epilepsy 显示文摘	Audenaert D Claes L Ceulemans B	2003	Neurology2003，61，6：	1
8	Effects of ozone exposure in open-top chambers on poplar (Populus nigra ) and beech ( Fagus sylvatica) : a comparison 显示文摘	Bortier K De Temmerman L Ceulemans R	2000	Environmental Pollution2000，109，3：	1
9	Symmetry-induced formation of antivortiees in mesoscopic superconductors显示文摘	CHIBOTARU L F CEULEMANS A BRUYNDONCX V	2000	Nature2000，408，：	1
10	De novo mutations in the sodium-channel gene SCN1A cause severe myoelonic epilepsy of infancy 显示文摘	Claes L Del-Favero J Ceulemans B	2001	Am J Hum Genet2001，68，6：	1
11	A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy显示文摘	Audenaert D Claes L Ceulemans B	2003	Neurology2003，61，6：	1
12	Evidence for the involve- ment of the glucocoticoid receptor gene in bipolar disorder in an i- solated northern Swedish population 显示文摘	Ceulemans S De Z S Heyrman L	2011	Bipolar Disord2011，13，78：	1
13	New insights in intestinal ischemia-reperfusion injury: implications for intestinal transplantation 显示文摘	LENAERTS K CEULEMAN L J HUNDSCHEID I H	2013	Curr Opin Organ Transplant2013，18，1：	1
14	De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy显示文摘	Claes L Ceulemans B Audenaert D	2003	Hum Mutat2003，21，6：	1
15	A deletion in SCNIB is associated with febrile seizures and early-onset absence epilepsy 显示文摘	Audenaert D Claes L Ceulemans B	2003	Neurology2003，61，6：	1
16	De novo SCN 1A mutation are a major cause of sever myoclonie epilepsy of infaney显示文摘	Laes L Ceulemans B Audenaert D	2003	Hum Mutat2003，21，6：	1
17	A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy显示文摘	Audenaert D Claes L Ceulemans B	2003	Neurology2003，61，：	1
18	Clinical correlations of mutations in the SCN1A gene: from febrile seizres to severe myoelonic epilepsy in infancy显示文摘	Ceulemans B Claes L Lagae L	2004	Pediatric neurology2004，30，4：	1
19	De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy 显示文摘	Claes L Del Favero J Ceulemans B	2001	Am J Hum Genet2001，68，6：	1
20	Clinical experience with levetiracetam in childhood epilepsy: an add-on and mono- therapy trial显示文摘	Lagae L Buyse G Ceulemans B	2005	Seizure2005，14，1：	1

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